DE60120109D1 - PROCESS FOR THE PREPARATION OF OPTIC-PURE (R) - AND (S) - DIDESMETHYLSIBUTRAMINE - Google Patents
PROCESS FOR THE PREPARATION OF OPTIC-PURE (R) - AND (S) - DIDESMETHYLSIBUTRAMINEInfo
- Publication number
- DE60120109D1 DE60120109D1 DE60120109T DE60120109T DE60120109D1 DE 60120109 D1 DE60120109 D1 DE 60120109D1 DE 60120109 T DE60120109 T DE 60120109T DE 60120109 T DE60120109 T DE 60120109T DE 60120109 D1 DE60120109 D1 DE 60120109D1
- Authority
- DE
- Germany
- Prior art keywords
- didesmethylsibutramine
- optic
- pure
- preparation
- racemic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- WQSACWZKKZPCHN-CQSZACIVSA-N (1r)-1-[1-(4-chlorophenyl)cyclobutyl]-3-methylbutan-1-amine Chemical compound C=1C=C(Cl)C=CC=1C1([C@H](N)CC(C)C)CCC1 WQSACWZKKZPCHN-CQSZACIVSA-N 0.000 title 1
- WQSACWZKKZPCHN-AWEZNQCLSA-N (1s)-1-[1-(4-chlorophenyl)cyclobutyl]-3-methylbutan-1-amine Chemical compound C=1C=C(Cl)C=CC=1C1([C@@H](N)CC(C)C)CCC1 WQSACWZKKZPCHN-AWEZNQCLSA-N 0.000 title 1
- UNAANXDKBXWMLN-UHFFFAOYSA-N sibutramine Chemical class C=1C=C(Cl)C=CC=1C1(C(N(C)C)CC(C)C)CCC1 UNAANXDKBXWMLN-UHFFFAOYSA-N 0.000 abstract 2
- 229940094659 Dopamine reuptake inhibitor Drugs 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000000221 dopamine uptake inhibitor Substances 0.000 abstract 1
- 239000002552 dosage form Substances 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C251/00—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton
- C07C251/02—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups
- C07C251/18—Compounds containing nitrogen atoms doubly-bound to a carbon skeleton containing imino groups having carbon atoms of imino groups bound to carbon atoms of rings other than six-membered aromatic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/11—Aldehydes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/10—Drugs for genital or sexual disorders; Contraceptives for impotence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/06—Antimigraine agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C211/00—Compounds containing amino groups bound to a carbon skeleton
- C07C211/01—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms
- C07C211/26—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring
- C07C211/29—Compounds containing amino groups bound to a carbon skeleton having amino groups bound to acyclic carbon atoms of an unsaturated carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by halogen atoms or by nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/44—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reduction and hydrolysis of nitriles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/38—Unsaturated compounds having —CHO groups bound to carbon atoms of rings other than six—membered aromatic rings
- C07C47/457—Unsaturated compounds having —CHO groups bound to carbon atoms of rings other than six—membered aromatic rings containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/04—Systems containing only non-condensed rings with a four-membered ring
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Pain & Pain Management (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Diabetes (AREA)
- Psychiatry (AREA)
- Obesity (AREA)
- Addiction (AREA)
- Gynecology & Obstetrics (AREA)
- Child & Adolescent Psychology (AREA)
- Reproductive Health (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Saccharide Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Methods of making and using racemic and optically pure metabolites of sibutramine, and pharmaceutically acceptable salts, solvates, and clathrates thereof, are disclosed. Pharmaceutical compositions and dosage forms are also disclosed which comprise a dopamine reuptake inhibitor, such as a racemic or optically pure sibutramine metabolite, and optionally an additional pharmacologically active compound.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/480,889 US6399826B1 (en) | 1999-08-11 | 2000-01-11 | Salts of sibutramine metabolites, methods of making sibutramine metabolites and intermediates useful in the same, and methods of treating pain |
| US480889 | 2000-01-11 | ||
| PCT/US2001/000762 WO2001051453A1 (en) | 2000-01-11 | 2001-01-10 | Racemic and optically pure metabolites of sibutramine, their preparation, compositions comprising them and their use as dopamine reuptake inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60120109D1 true DE60120109D1 (en) | 2006-07-06 |
| DE60120109T2 DE60120109T2 (en) | 2006-10-19 |
Family
ID=23909753
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60120109T Expired - Fee Related DE60120109T2 (en) | 2000-01-11 | 2001-01-10 | METHOD FOR THE PRODUCTION OF OPTICALLY PURE (R) - AND (S) - DIDESMETHYLSIBUTRAMINE |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US6399826B1 (en) |
| EP (2) | EP1632471A1 (en) |
| JP (1) | JP2003519675A (en) |
| AT (1) | ATE327972T1 (en) |
| AU (1) | AU782567B2 (en) |
| CA (1) | CA2396950A1 (en) |
| CY (1) | CY1106150T1 (en) |
| DE (1) | DE60120109T2 (en) |
| DK (1) | DK1246789T3 (en) |
| ES (1) | ES2260195T3 (en) |
| PT (1) | PT1246789E (en) |
| WO (1) | WO2001051453A1 (en) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6974838B2 (en) * | 1998-08-24 | 2005-12-13 | Sepracor Inc. | Methods of treating or preventing pain using sibutramine metabolites |
| US6476078B2 (en) * | 1999-08-11 | 2002-11-05 | Sepracor, Inc. | Methods of using sibutramine metabolites in combination with a phosphodiesterase inhibitor to treat sexual dysfunction |
| KR20030077538A (en) * | 2000-11-15 | 2003-10-01 | 탭 파마슈티칼 프로덕츠 인코포레이티드 | Treatment of anti-depression drug-induced sexual dysfunction with apomorphine |
| US20050192271A1 (en) * | 2003-07-15 | 2005-09-01 | Hythiam, Inc. | Use of selective chloride channel modulators to treat alcohol and/or stimulant substance abuse |
| CN1659154B (en) * | 2002-04-10 | 2012-05-30 | 艾普辛特姆有限责任公司 | Preparation method of amine stereoisomer |
| RU2290924C2 (en) * | 2002-10-05 | 2007-01-10 | Ханми Фарм. Ко., Лтд. | Pharmaceutical composition including crystalline sibutramine methanesulfonate hemihydrate |
| KR100536750B1 (en) * | 2002-10-05 | 2005-12-16 | 한미약품 주식회사 | Pharmaceutical composition comprising crystalline hemihydrate of sibutramine methanesulfonate |
| CL2004000826A1 (en) * | 2003-04-25 | 2005-03-04 | Pfizer | USE OF AN AGONIST FOR THE 5-HT2C RECEPTOR TO PREPARE A USEFUL MEDICINAL PRODUCT IN THE TREATMENT OF URINARY INCONTINENCE CAUSED BY STRESS, WITH THE CONDITION THAT THE AGONIST IS NOT 1- [6-CHLORINE-5- (TRIFLUOROMETIL) -2- PIRIDINIL] PIPERAZINA (ORG-129 |
| WO2005041988A1 (en) * | 2003-10-22 | 2005-05-12 | University Of Florida | Method and composition for pain amelioration |
| US20050209220A1 (en) * | 2004-03-19 | 2005-09-22 | Jeffrey Conforti | Treatment of peripheral neuropathy |
| US20060160905A1 (en) * | 2005-01-18 | 2006-07-20 | Bergeron Raymond J Jr | Compositions and methods for inhibiting pain |
| EP1851190A4 (en) | 2005-01-18 | 2009-04-08 | Univ Florida | PREPARATIONS AND METHODS OF INHIBITING PAIN |
| US8604244B2 (en) | 2010-07-02 | 2013-12-10 | Reviva Pharmaceuticals, Inc. | Compositions, synthesis, and methods of using cycloalkylmethylamine derivatives |
| JP2010503709A (en) | 2006-09-15 | 2010-02-04 | レビバ ファーマシューティカルズ,インコーポレーテッド | Synthesis, methods of use and compositions of cycloalkylmethylamines |
| CN101555214B (en) | 2008-04-08 | 2012-07-11 | 北京嘉事联博医药科技有限公司 | Phenylcyclobutylamide derivatives and optical isomers, preparation methods and uses thereof |
| WO2010065889A2 (en) * | 2008-12-06 | 2010-06-10 | Auspex Pharmaceutical | Cyclobutanemethanamine inhibitors of monomine reuptake |
| CN102791134B (en) | 2009-12-04 | 2015-04-22 | 魄金莱默有限公司 | Method of using dopamine reuptake inhibitors and their analogs for treating diabetes symptoms and delaying or preventing diabetes-associated pathologic conditions |
| CN104039753B (en) | 2011-12-30 | 2016-09-14 | 雷维瓦药品公司 | The compositions of phenylcycloalkyl methylamine derivative, synthesis and using method |
| GB202114564D0 (en) * | 2021-10-12 | 2021-11-24 | Actimed Therapeutics Ltd | Oral formulation |
Family Cites Families (63)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3155670A (en) | 1962-06-22 | 1964-11-03 | Res Lab Dr C Janssen N V | 1-oxo-2, 4, 8, triaza-spiro (4, 5) decanes |
| US3155669A (en) | 1962-06-22 | 1964-11-03 | Res Lab Dr C Janssen N V | 2, 4, 8-triaza-spiro (4, 5) dec-2-enes |
| US3471515A (en) | 1965-02-01 | 1969-10-07 | Sandoz Ag | (2-hydroxy-3-substituted aminopropoxy)indoles |
| US3536809A (en) | 1969-02-17 | 1970-10-27 | Alza Corp | Medication method |
| US3598123A (en) | 1969-04-01 | 1971-08-10 | Alza Corp | Bandage for administering drugs |
| GB1308191A (en) | 1970-04-06 | 1973-02-21 | Science Union & Cie | Thiochroman derivatives and a process for preparing them |
| US3845770A (en) | 1972-06-05 | 1974-11-05 | Alza Corp | Osmatic dispensing device for releasing beneficial agent |
| US3916899A (en) | 1973-04-25 | 1975-11-04 | Alza Corp | Osmotic dispensing device with maximum and minimum sizes for the passageway |
| US4008719A (en) | 1976-02-02 | 1977-02-22 | Alza Corporation | Osmotic system having laminar arrangement for programming delivery of active agent |
| DE3008993A1 (en) | 1980-03-08 | 1981-10-01 | Röhm Pharma GmbH, 6100 Darmstadt | PHARMACEUTICAL PREPARATIONS |
| ZA821577B (en) | 1981-04-06 | 1983-03-30 | Boots Co Plc | Therapeutic agents |
| IE52768B1 (en) | 1981-04-06 | 1988-02-17 | Boots Co Ltd | 1-arylcyclobutylalkylamine compounds useful as therapeutic agents |
| JPS5940638A (en) | 1982-08-30 | 1984-03-06 | Fuji Photo Film Co Ltd | Silver halide photographic emulsion for direct positive |
| IE58110B1 (en) | 1984-10-30 | 1993-07-14 | Elan Corp Plc | Controlled release powder and process for its preparation |
| GB8501192D0 (en) * | 1985-01-17 | 1985-02-20 | Boots Co Plc | Therapeutic agents |
| GB8531071D0 (en) | 1985-12-17 | 1986-01-29 | Boots Co Plc | Therapeutic compound |
| GB8704777D0 (en) | 1987-02-28 | 1987-04-01 | Boots Co Plc | Medical treatment |
| JP2675573B2 (en) | 1988-03-31 | 1997-11-12 | 科研製薬株式会社 | Brain function improver |
| US5073543A (en) | 1988-07-21 | 1991-12-17 | G. D. Searle & Co. | Controlled release formulations of trophic factors in ganglioside-lipsome vehicle |
| IE61928B1 (en) | 1988-11-29 | 1994-11-30 | Boots Co Plc | Treatment of obesity |
| GB8909209D0 (en) | 1989-04-22 | 1989-06-07 | Wyeth John & Brother Ltd | Piperazine derivatives |
| IT1229203B (en) | 1989-03-22 | 1991-07-25 | Bioresearch Spa | USE OF 5 METHYLTHETRAHYDROPHOLIC ACID, 5 FORMYLTHETRAHYDROPHOLIC ACID AND THEIR PHARMACEUTICALLY ACCEPTABLE SALTS FOR THE PREPARATION OF PHARMACEUTICAL COMPOSITIONS IN THE FORM OF CONTROLLED RELEASE ACTIVE IN THE THERAPY OF MENTAL AND ORGANIC DISORDERS. |
| US5120548A (en) | 1989-11-07 | 1992-06-09 | Merck & Co., Inc. | Swelling modulated polymeric drug delivery device |
| US5733566A (en) | 1990-05-15 | 1998-03-31 | Alkermes Controlled Therapeutics Inc. Ii | Controlled release of antiparasitic agents in animals |
| US5250534A (en) | 1990-06-20 | 1993-10-05 | Pfizer Inc. | Pyrazolopyrimidinone antianginal agents |
| US5104899A (en) | 1990-08-13 | 1992-04-14 | Sepracor, Inc. | Methods and compositions for treating depression using optically pure fluoxetine |
| US5580578A (en) | 1992-01-27 | 1996-12-03 | Euro-Celtique, S.A. | Controlled release formulations coated with aqueous dispersions of acrylic polymers |
| EP0554172B1 (en) | 1992-01-28 | 1998-04-29 | Fujitsu Limited | Color surface discharge type plasma display device |
| US5780051A (en) | 1992-04-02 | 1998-07-14 | Dynagen, Inc. | Methods and articles of manufacture for nicotine cessation and monitoring nicotine use |
| CA2139000A1 (en) | 1992-06-23 | 1994-01-06 | James W. Young | Methods and compositions for treating depression and other disorders using optically pure(+) sibutramine |
| CA2138998A1 (en) | 1992-06-23 | 1994-01-06 | James W. Young | Methods and compositions for treating depression and other disorders using optically pure(-) sibutramine |
| US5591767A (en) | 1993-01-25 | 1997-01-07 | Pharmetrix Corporation | Liquid reservoir transdermal patch for the administration of ketorolac |
| GB9301192D0 (en) | 1993-06-09 | 1993-06-09 | Trott Francis W | Flower shaped mechanised table |
| US5459164A (en) | 1994-02-03 | 1995-10-17 | Boots Pharmaceuticals, Inc. | Medical treatment |
| GB9402641D0 (en) | 1994-02-11 | 1994-04-06 | Boots Co Plc | Therapeutic agents |
| CA2134038C (en) | 1994-06-16 | 1997-06-03 | David Taiwai Wong | Potentiation of drug response |
| ATE212860T1 (en) | 1994-09-19 | 2002-02-15 | Fujisawa Pharmaceutical Co | A NOVEL MEDICAL USE OF A 5HT 3 ANTAGONIST |
| GB9514464D0 (en) | 1995-07-14 | 1995-09-13 | Glaxo Lab Sa | Medicaments |
| GB9524681D0 (en) | 1995-12-02 | 1996-01-31 | Knoll Ag | Chemical process |
| DE19632423A1 (en) | 1996-08-12 | 1998-02-19 | Merck Patent Gmbh | Thienopyrimidines |
| GB9619757D0 (en) | 1996-09-21 | 1996-11-06 | Knoll Ag | Chemical process |
| GB9619961D0 (en) | 1996-09-25 | 1996-11-13 | Knoll Ag | Medical treatment |
| GB9619962D0 (en) | 1996-09-25 | 1996-11-13 | Knoll Ag | Medical treatment |
| US5795880A (en) | 1996-12-30 | 1998-08-18 | Louisiana State University Medical Center Foundation | Method and composition for treating obesity and related disorders in animals comprising dehydroepiandrosterone (DHEA), or a derivative thereof, and an anorectic agent |
| US6127363A (en) | 1997-10-28 | 2000-10-03 | Vivus, Inc. | Local administration of Type IV phosphodiesterase inhibitors for the treatment of erectile dysfunction |
| GB9727131D0 (en) | 1997-12-24 | 1998-02-25 | Knoll Ag | Therapeutic agents |
| GB2340037A (en) | 1998-07-30 | 2000-02-16 | Glaxo Group Ltd | Compositions comprising bupropion for the treatment of premature ejaculation |
| US6331571B1 (en) * | 1998-08-24 | 2001-12-18 | Sepracor, Inc. | Methods of treating and preventing attention deficit disorders |
| US6046242A (en) | 1998-11-27 | 2000-04-04 | Basf Aktiengesellschaft | Use of aryl-substituted cyclobutylalkylamines for treating urinary incontinence |
| WO2000056148A1 (en) | 1999-03-19 | 2000-09-28 | Knoll Pharmaceutical Company | Treatment of pharmacology of drug misuse and other addictive disorders |
| IL145244A (en) | 1999-03-19 | 2006-12-10 | Abbott Gmbh & Co Kg | Method of treating sleep apnoea |
| WO2000056320A1 (en) | 1999-03-19 | 2000-09-28 | Knoll Pharmaceutical Company | Treatment of menstrual function |
| AU3759800A (en) | 1999-03-19 | 2000-10-09 | Knoll Pharmaceutical Company | Treatment of premenstrual syndrome |
| AU3898600A (en) | 1999-03-19 | 2000-10-09 | Knoll Pharmaceutical Company | Method of treating obsessive-compulsive disorder |
| WO2000056318A1 (en) | 1999-03-19 | 2000-09-28 | Knoll Pharmaceutical Company | Treatment of neuropathic pain or fibromyalgia |
| EP1178790A1 (en) | 1999-03-19 | 2002-02-13 | Knoll GmbH | Treatment to lower platelet adhesiveness |
| PL351963A1 (en) | 1999-03-19 | 2003-07-14 | Knoll Gmbh | Method of treating eating disorders |
| WO2000056309A1 (en) | 1999-03-19 | 2000-09-28 | Knoll Pharmaceutical Company | Method of treating sexual dysfunction |
| AU3899100A (en) | 1999-03-19 | 2000-10-09 | Knoll Pharmaceutical Company | Treatment of hyperactivity disorders |
| US6376553B1 (en) * | 1999-03-19 | 2002-04-23 | Knoll Pharmaceutical Company | Treatment of pain |
| WO2000056149A1 (en) | 1999-03-19 | 2000-09-28 | Knoll Pharmaceutical Company | Method of treating anxiety disorders |
| CZ20013284A3 (en) | 1999-03-19 | 2002-10-16 | Knoll Gmbh | Pharmaceutical composition intended for treating osteoarthritis or holarthritis |
| GB9914742D0 (en) * | 1999-06-24 | 1999-08-25 | Knoll Ag | Therapeutic agents |
-
2000
- 2000-01-11 US US09/480,889 patent/US6399826B1/en not_active Expired - Fee Related
-
2001
- 2001-01-10 DE DE60120109T patent/DE60120109T2/en not_active Expired - Fee Related
- 2001-01-10 CA CA002396950A patent/CA2396950A1/en not_active Abandoned
- 2001-01-10 JP JP2001551835A patent/JP2003519675A/en active Pending
- 2001-01-10 AU AU27793/01A patent/AU782567B2/en not_active Ceased
- 2001-01-10 PT PT01901941T patent/PT1246789E/en unknown
- 2001-01-10 EP EP05108783A patent/EP1632471A1/en not_active Withdrawn
- 2001-01-10 EP EP01901941A patent/EP1246789B1/en not_active Expired - Lifetime
- 2001-01-10 ES ES01901941T patent/ES2260195T3/en not_active Expired - Lifetime
- 2001-01-10 WO PCT/US2001/000762 patent/WO2001051453A1/en not_active Ceased
- 2001-01-10 DK DK01901941T patent/DK1246789T3/en active
- 2001-01-10 AT AT01901941T patent/ATE327972T1/en not_active IP Right Cessation
-
2002
- 2002-06-04 US US10/160,033 patent/US6710087B2/en not_active Expired - Fee Related
-
2006
- 2006-08-30 CY CY20061101224T patent/CY1106150T1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU782567B2 (en) | 2005-08-11 |
| WO2001051453A1 (en) | 2001-07-19 |
| JP2003519675A (en) | 2003-06-24 |
| CA2396950A1 (en) | 2001-07-19 |
| CY1106150T1 (en) | 2011-06-08 |
| US20020183281A1 (en) | 2002-12-05 |
| EP1246789B1 (en) | 2006-05-31 |
| DK1246789T3 (en) | 2006-09-18 |
| EP1632471A1 (en) | 2006-03-08 |
| AU2779301A (en) | 2001-07-24 |
| ATE327972T1 (en) | 2006-06-15 |
| ES2260195T3 (en) | 2006-11-01 |
| US6710087B2 (en) | 2004-03-23 |
| DE60120109T2 (en) | 2006-10-19 |
| PT1246789E (en) | 2006-10-31 |
| EP1246789A1 (en) | 2002-10-09 |
| US6399826B1 (en) | 2002-06-04 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| DE60120109D1 (en) | PROCESS FOR THE PREPARATION OF OPTIC-PURE (R) - AND (S) - DIDESMETHYLSIBUTRAMINE | |
| MXPA05009367A (en) | Opioid receptor antagonists. | |
| DK1663206T3 (en) | 1- (2,3-Dimethyl-phenyl) -ethyl-1,3-dihydro-imizadol-2-thione as a non-sedative alpha 2A agonist | |
| NO20071498L (en) | Substituted acyl hydroxamic acids as well as methods for reducing the TNFα level | |
| ZA200700765B (en) | Nebivolol and its pharmaceutically acceptable salts, process for preparation and pharmaceutical compositions of nebivolol | |
| HUP0300301A2 (en) | New aminopropylphosphinic acids | |
| EA200300999A1 (en) | CHRONOTHERAPEUTIC DOSED FORMS | |
| EA201200954A1 (en) | METHOD OF OBTAINING HYDROCHLORIDE (R) -8-CHLOR-1-METHYL-HALT-HYDROCHLORIDE (R) -8-CHLOR-1-METHYL-2,3,4,5-TETRAHYDRO-1H-3-BENZAZEPINA, PHARMACEUTICAL COMPOSITION ON ITS BASIS AND ITS APPLICATION | |
| CY1106682T1 (en) | LAKTAMIS ASSOCIATION | |
| DE602004005323D1 (en) | AZID-FREE PROCESS FOR THE PREPARATION OF 1,2-DIAMINO COMPOUNDS | |
| ATE308522T1 (en) | OPIOID RECEPTOR ANTAGONISTS | |
| BR0209554A (en) | Methods for preparing a compound, and compound | |
| ATE466008T1 (en) | P-GLYCOPROTEIN INHIBITOR, METHOD FOR PRODUCING THEREOF AND PHARMACEUTICAL COMPOSITION CONTAINING SAME | |
| EA200500690A1 (en) | NEW PYRIDOPYRIMIDINON COMPOUNDS, METHOD OF THEIR PRODUCTION AND PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM | |
| CY1107473T1 (en) | A PYRIDINE-N-OXIDE PRODUCER, AND THE PROCEDURE FOR TRANSFERING ITS EFFECTIVE PHARMACEUTICAL COMPOSITIONS | |
| MY138826A (en) | 2,7-substituted indoles | |
| WO2001081316A3 (en) | Substituted phenyl farnesyltransferase inhibitors | |
| EA200701687A1 (en) | Amorphous hydrochloride lorkanidipine | |
| EA200300272A1 (en) | NEW HINAZOLIN DERIVATIVES, METHOD OF THEIR PRODUCTION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM | |
| BRPI0411293A8 (en) | COMPOUND, PHARMACEUTICAL COMPOSITION, PROCESS FOR PREPARING A COMPOUND, AND USE OF A COMPOUND | |
| FI20077133A7 (en) | Escitalopram crystalline base and escitalopram base orodispersible tablets | |
| ATE469887T1 (en) | SUBSTITUTED HETEROCYCLIC COMPOUNDS AND THEIR USE FOR TREATING MULTIPLE DRUG RESISTANCE | |
| DE60238251D1 (en) | RESOLUTION METHOD FOR THE PREPARATION OF (R) - (-) - 2-HYDROXY-2- (2-CHLOROPHENYL) ACETIC ACID | |
| MXPA02004538A (en) | 3-amino-1-indanole, method of synthesizing the same and method of optical resolution. | |
| NO20030876D0 (en) | Process for racemization of 1-benzyl-4- (4-fluorophenyl) -3-hydroxymethyl-1,2,3,6-tetrahydropyridine for use as an intermediate in the synthesis of paroxetine |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |